Literature DB >> 8504018

A risk-benefit assessment of tamoxifen therapy.

W H Catherino1, V C Jordan.   

Abstract

Tamoxifen is the endocrine treatment of choice for all women with hormonally responsive breast cancer. 30 years of experience in both the laboratory and clinical setting have shown tamoxifen to be an effective adjuvant treatment with minor short term adverse effects. However, as therapeutic use has extended to 5 years and beyond, and as clinical trials begin which will assess the effectiveness of tamoxifen as a preventive treatment, concern about possible long term adverse effects is justified. Tamoxifen has an estrogen-like influence on the skeletal and cardiovascular systems, resulting in decreases in both postmenopausal bone loss and low density lipoprotein (LDL) levels. These effects will, it is hoped, result in decreases in the incidences of osteoporosis and coronary heart disease, which are major causes of morbidity and mortality in the postmenopausal age group. Tamoxifen therapy also results in decreased rates of contralateral breast cancer. Long term tamoxifen treatment may result in a small increase in the incidence of endometrial and/or hepatocellular carcinoma, but with millions of women taking tamoxifen for long periods, such small increases in incidence translate to a significant number of women at risk. Tamoxifen is clearly beneficial for short term treatment, but the clinical decision of tamoxifen use in the long term must be made on the individual benefits versus risks of tamoxifen treatment.

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Year:  1993        PMID: 8504018     DOI: 10.2165/00002018-199308050-00005

Source DB:  PubMed          Journal:  Drug Saf        ISSN: 0114-5916            Impact factor:   5.606


  149 in total

1.  Tamoxifen-associated hepatocellular damage and agranulocytosis.

Authors:  C K Ching; P G Smith; R G Long
Journal:  Lancet       Date:  1992-04-11       Impact factor: 79.321

2.  Effects of anti-estrogens on bone in castrated and intact female rats.

Authors:  V C Jordan; E Phelps; J U Lindgren
Journal:  Breast Cancer Res Treat       Date:  1987-10       Impact factor: 4.872

3.  Comparison between tamoxifen and clomiphene therapy in women with anovulation.

Authors:  I Gerhard; B Runnebaum
Journal:  Arch Gynecol       Date:  1979

4.  Tamoxifen as risk factor for carcinoma of corpus uteri.

Authors:  L Hardell
Journal:  Lancet       Date:  1988-09-03       Impact factor: 79.321

5.  Tamoxifen and arterial thrombosis.

Authors:  R Dahan; M Espie; L Mignot; D Houlbert; B Chanu
Journal:  Lancet       Date:  1985-03-16       Impact factor: 79.321

Review 6.  The pharmacology and clinical uses of tamoxifen.

Authors:  B J Furr; V C Jordan
Journal:  Pharmacol Ther       Date:  1984       Impact factor: 12.310

7.  Transforming growth factors type beta 1 and beta 2 are equipotent growth inhibitors of human breast cancer cell lines.

Authors:  G Zugmaier; B W Ennis; B Deschauer; D Katz; C Knabbe; G Wilding; P Daly; M E Lippman; R B Dickson
Journal:  J Cell Physiol       Date:  1989-11       Impact factor: 6.384

8.  Tamoxifen treatment of metastatic breast cancer and antithrombin III levels.

Authors:  R E Enck; C N Rios
Journal:  Cancer       Date:  1984-06-15       Impact factor: 6.860

9.  Determination and pharmacology of a new hydroxylated metabolite of tamoxifen observed in patient sera during therapy for advanced breast cancer.

Authors:  V C Jordan; R R Bain; R R Brown; B Gosden; M A Santos
Journal:  Cancer Res       Date:  1983-03       Impact factor: 12.701

10.  Antitumor actions of toremifene in the 7,12-dimethylbenzanthracene (DMBA)-induced rat mammary tumor model.

Authors:  S P Robinson; D A Mauel; V C Jordan
Journal:  Eur J Cancer Clin Oncol       Date:  1988-12
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  8 in total

1.  Effects of tamoxifen on bone mineral density and metabolism in postmenopausal women with early-stage breast cancer.

Authors:  Jamal Zidan; Zohar Keidar; Walid Basher; Ora Israel
Journal:  Med Oncol       Date:  2004       Impact factor: 3.064

Review 2.  Tamoxifen: a review of pharmacoeconomic and quality-of-life considerations for its use as adjuvant therapy in women with breast cancer.

Authors:  H M Bryson; G L Plosker
Journal:  Pharmacoeconomics       Date:  1993-07       Impact factor: 4.981

3.  Apoptosis and tumorigenesis in human cholangiocarcinoma cells. Involvement of Fas/APO-1 (CD95) and calmodulin.

Authors:  G Pan; S M Vickers; A Pickens; J O Phillips; W Ying; J A Thompson; G P Siegal; J M McDonald
Journal:  Am J Pathol       Date:  1999-07       Impact factor: 4.307

4.  Effects of tamoxifen on serum lipid and apolipoprotein levels in postmenopausal patients with breast cancer.

Authors:  M Morales; N Santana; A Soria; A Mosquera; J Ordovás; J Nóvoa; P Betancor; P F Valerón; B Díaz-Chico; R Chirino
Journal:  Breast Cancer Res Treat       Date:  1996       Impact factor: 4.872

5.  Long term adjuvant therapy for primary breast cancer.

Authors:  R D Bulbrook
Journal:  BMJ       Date:  1996-02-17

Review 6.  Comparative tolerability of first-generation selective estrogen receptor modulators in breast cancer treatment and prevention.

Authors:  M G Curtis
Journal:  Drug Saf       Date:  2001       Impact factor: 5.606

7.  Tamoxifen and risk of idiopathic venous thromboembolism.

Authors:  C R Meier; H Jick
Journal:  Br J Clin Pharmacol       Date:  1998-06       Impact factor: 4.335

8.  Long-term follow-up of elderly patients with operable breast cancer treated with surgery without axillary dissection plus adjuvant tamoxifen.

Authors:  G Martelli; G DePalo; N Rossi; D Coradini; P Boracchi; E Galante; G Vetrella
Journal:  Br J Cancer       Date:  1995-11       Impact factor: 7.640

  8 in total

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